HuGE Literature Finder
Records 1-11
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A pilot Indian family-based association study between dyslexia and Reelin pathway genes, DCDC2 and ROBO1, identifies modest association with a triallelic unit TAT in the gene RELN.
Asian journal of psychiatry 2018 Aug 37 121-129. Devasenapathy Subhashree, Midha Rashi, Naskar Teesta, Mehta Anuradha, Prajapati Bharat, Ummekulsum Mariam, Sagar Rajesh, Singh Nandini C, Sinha Subra |
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Genome-wide investigation of schizophrenia associated plasma Ndel1 enzyme activity.
Schizophrenia research 2016 Feb . Gadelha Ary, Coleman Jonathan, Breen Gerome, Mazzoti Diego Robles, Yonamine Camila M, Pellegrino Renata, Ota Vanessa Kiyomi, Belangero Sintia Iole, Glessner Joseph, Sleiman Patrick, Hakonarson Hakon, Hayashi Mirian A F, Bressan Rodrigo |
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[Association of gene polymorphisms with the susceptibility of schizophrenia in Han Chinese population].
Zhonghua yi xue za zhi 2015 Dec 95 (47): 3803-7. Yu Hongyan, Zhang Haisan, Yang Yongfeng, Li Wenqiang, Zhang Hongxing, Yang Ge, Lü Luxi |
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Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.
Molecular psychiatry 2014 Aug 19 (8): 872-9. Kenny E M, Cormican P, Furlong S, Heron E, Kenny G, Fahey C, Kelleher E, Ennis S, Tropea D, Anney R, Corvin A P, Donohoe G, Gallagher L, Gill M, Morris D |
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No association of polymorphisms in the CDK5, NDEL1, and LIS1 with autism in Chinese Han population.
Psychiatry research 2011 Dec 190 (2-3): 369-71. Wang Lifang, Li Jun, Jia Meixiang, Yue Weihua, Ruan Yanyan, Lu Tianlan, Zhang Jishui, Liu Jing, Zhang D |
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Interaction between FEZ1 and DISC1 in regulation of neuronal development and risk for schizophrenia.
Neuron 2011 Nov 72 (4): 559-71. Kang Eunchai, Burdick Katherine E, Kim Ju Young, Duan Xin, Guo Junjie U, Sailor Kurt A, Jung Dhong-Eun, Ganesan Sundar, Choi Sungkyung, Pradhan Dennis, Lu Bai, Avramopoulos Dimitrios, Christian Kimberly, Malhotra Anil K, Song Hongjun, Ming Guo- |
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Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.
PloS one 2011 6 (8): e23450. Moens Lotte N, De Rijk Peter, Reumers Joke, Van den Bossche Maarten J A, Glassee Wim, De Zutter Sonia, Lenaerts An-Sofie, Nordin Annelie, Nilsson Lars-Göran, Medina Castello Ignacio, Norrback Karl-Fredrik, Goossens Dirk, Van Steen Kristel, Adolfsson Rolf, Del-Favero Jurg |
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Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging.
Human genetics 2010 Apr 127 (4): 441-52. Nicodemus Kristin K, Callicott Joseph H, Higier Rachel G, Luna Augustin, Nixon Devon C, Lipska Barbara K, Vakkalanka Radhakrishna, Giegling Ina, Rujescu Dan, St Clair David, Muglia Pierandrea, Shugart Yin Yao, Weinberger Daniel |
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Genetic association and post-mortem brain mRNA analysis of DISC1 and related genes in schizophrenia.
Schizophrenia research 2009 Oct 114 (1-3): 39-49. Rastogi Anjali, Zai Clement, Likhodi Olga, Kennedy James L, Wong Albert |
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Association between genes of Disrupted in schizophrenia 1 (DISC1) interactors and schizophrenia supports the role of the DISC1 pathway in the etiology of major mental illnesses.
Biological psychiatry 2009 Jun 65 (12): 1055-62. Tomppo Liisa, Hennah William, Lahermo Päivi, Loukola Anu, Tuulio-Henriksson Annamari, Suvisaari Jaana, Partonen Timo, Ekelund Jesper, Lönnqvist Jouko, Peltonen Lee |
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Elucidating the relationship between DISC1, NDEL1 and NDE1 and the risk for schizophrenia: evidence of epistasis and competitive binding.
Human molecular genetics 2008 Aug 17 (16): 2462-73. Burdick Katherine E, Kamiya Atsushi, Hodgkinson Colin A, Lencz Todd, DeRosse Pamela, Ishizuka Koko, Elashvili Sarah, Arai Hiroyuki, Goldman David, Sawa Akira, Malhotra Anil |
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- Page last updated:Jan 23, 2020
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